A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9672746



Internal ID14911248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89224970..89224989hg38UCSC Ensembl
Innerchr16:89224966..89224993hg38UCSC Ensembl
Outerchr16:89224947..89225012hg38UCSC Ensembl
chr16:89291378..89291397hg19UCSC Ensembl
Innerchr16:89291374..89291401hg19UCSC Ensembl
Outerchr16:89291355..89291420hg19UCSC Ensembl
chr16:87818879..87818898hg18UCSC Ensembl
Innerchr16:87818902..87818875hg18UCSC Ensembl
Outerchr16:87818856..87818921hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38300
hg19300
hg18300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3441548
Supporting Variants
SamplesNA19141
Known GenesZNF778
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv9672746
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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